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… in the EU and the Inflation Reduction Act (IRA) in the US Anne Heyes, MBA Vice President, Head of Value & Access , … new Medicare Drug Price Negotiation Program. The European regulation on health technology assessment is due to be … therapies (also known as cell and gene therapies), and medical technologies. Therapies for rare diseases will be …
… NETHERLANDS PHARMO Institute Utrecht University University Medical Center Utrecht University Medical Center Groningen SPAIN Aragon Institute of Public … Valencia Region (FISABIO) Spanish Agency of Medicines and Medical Devices (AEMPS) Spanish Center for …
… research can help you gain insights on: Medication, device, vaccine, and other treatment safety profiles Disease … studies for pharmaceutical clients at the request of the US FDA, EMA, and other national agencies in North America, … conducted research in populations covered by electronic medical records, administrative claims, and registries for …
… real-world evidence (RWE) at every stage of your drug or device development journey. Experienced Real-World Data Analysis for Medical Product Research Our experts have collected and … can help you understand what RWE guidelines mean for your medical product research and development. You can have …
… Medical Technologies Chart a complete course to commercial … Our experts can help you justify the value of your medical device, diagnostic, or digital technology to …
… the question, “Does the choice of a respondent’s device adversely affect choice behavior or data quality?” The differences between PC and mobile device experiences are well known. While data collection … The goal of this study was to understand if the device type used affected these seven parameters: Drop-out …
… important for reimbursement decisions in both the US and many European countries as risks and benefits, … within the industry. Grounded in science and supported by state-of-the-art technology, we can help you develop …
… by European regulators were often conducted in the US. ENCePP filled a need by creating a network to facilitate … future, ENCePP will need to be innovative in addressing current challenges such as data protection concerns, …
… Recent FDA Drug and Device Guidelines for Sharing Pre-Approval Information Share … by Drug and Device Manufacturers to Payers in the US In the US, once a drug or medical device has been approved or received clearance, …
… Medical Writing, Editing, and Design Services …